FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Velocity

K Number: K173636 · Decision Feb 15, 2018
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
49
Review Days
83

Basic Information

Device Name
Velocity
K Number
K173636
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Varian Medical Systems, Inc.
Date Received
November 24, 2017
Decision Date
February 15, 2018
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLZ System, Image Processing, Radiological

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